Evidence map›Paper›PMID 20336144›Full record

ArticleNature2010

Primary contribution to zebrafish heart regeneration by gata4(+) cardiomyocytes.

Kazu Kikuchi, Jennifer E Holdway, Andreas A Werdich, Ryan M Anderson, Yi Fang, Gregory F Egnaczyk, Todd Evans, Calum A Macrae, Didier Y R Stainier, Kenneth D Poss

Open access · greenAbstract read
In one paragraph

Article in Nature, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 618 papers.

0numbers the graph read from it
0cells of the map it votes in
618citing papers in PubMed
34.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

618 citing papers in PubMed, 1,055 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Signaling pathways regulating cardiac regeneration.Cell regeneration (London, England) · 2026
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Molecular evolution of animal aging.The EMBO journal · 2026
    Review
  19. Review
  20. Hb-EGF directs systemic muscle repair.Development (Cambridge, England) · 2026
    Article

558 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Kazu KikuchiDepartment of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Jennifer E Holdway
Andreas A Werdich
Ryan M Anderson
Yi Fang
Gregory F Egnaczyk
Todd Evans
Calum A Macrae
Didier Y R Stainier
Kenneth D Poss
Brigham and Women's Hospital · USHoward Hughes Medical Institute · USInstitute of Cell Biology · UAUniversity of California, San Francisco · USCornell University · USDuke University · US

Funding

MULTIDISCIPLINARY RESEARCH TRAINING IN CARDIOLOGYT32HL007208 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Patrick Thomas Ellinor, David E Sosnovik · 1985 to 2026
$16.1M
MULTIDISCIPLINARY HEART &VASCULAR DISEASEST32HL007101 · NHLBI · DUKE UNIVERSITY · PI FREEDMAN, NEIL J. · 1985 to 2020
$9.8M
Regulation of Myocardial Regeneration in ZebrafishR01HL081674 · NHLBI · DUKE UNIVERSITY · PI POSS, KENNETH D · 2005 to 2019
$6.6M
MOLECULAR GENETICS OF CARDIAC CELL DIFFERENTIATIONR01HL054737 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COUGHLIN, SHAUN R. · 1996 to 2015
$5.4M
Function of GATA Factors in CardiogenesisR01HL064282 · NHLBI · YESHIVA UNIVERSITY · PI EVANS, TODD R · 2000 to 2008
$3.5M
Zebrafish Assays Predictive for Cardiotoxicity(RMI)R21GM075946 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI MACRAE, CALUM A. · 2005 to 2008
$1.6M
Development of a High-throughput Integrated In Vivo Heart Failure AssayR01HL109264 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MACRAE, CALUM A. · 2012 to 2014
$1.3M
Genetic Studies of Cardiac Pacemaking in the ZebrafishK08HL068711 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MACRAE, CALUM A. · 2002 to 2004
$383k
Howard Hughes Medical InstituteNHLBI NIH HHS HL007101NHLBI NIH HHS HL007208NHLBI NIH HHS HL054737NHLBI NIH HHS HL064282NHLBI NIH HHS HL081674NHLBI NIH HHS R01 HL054737NHLBI NIH HHS R01 HL064282NHLBI NIH HHS R01 HL081674NHLBI NIH HHS R01 HL109264NHLBI NIH HHS T32 HL007101NHLBI NIH HHS T32 HL007208NIGMS NIH HHS GM075846NIGMS NIH HHS R21 GM075946
6 · The paper itself

Abstract

Recent studies indicate that mammals, including humans, maintain some capacity to renew cardiomyocytes throughout postnatal life. Yet, there is little or no significant cardiac muscle regeneration after an injury such as acute myocardial infarction. By contrast, zebrafish efficiently regenerate lost cardiac muscle, providing a model for understanding how natural heart regeneration may be blocked or enhanced. In the absence of lineage-tracing technology applicable to adult zebrafish, the cellular origins of newly regenerated cardiac muscle have remained unclear. Using new genetic fate-mapping approaches, here we identify a population of cardiomyocytes that become activated after resection of the ventricular apex and contribute prominently to cardiac muscle regeneration. Through the use of a transgenic reporter strain, we found that cardiomyocytes throughout the subepicardial ventricular layer trigger expression of the embryonic cardiogenesis gene gata4 within a week of trauma, before expression localizes to proliferating cardiomyocytes surrounding and within the injury site. Cre-recombinase-based lineage-tracing of cells expressing gata4 before evident regeneration, or of cells expressing the contractile gene cmlc2 before injury, each labelled most cardiac muscle in the ensuing regenerate. By optical voltage mapping of surface myocardium in whole ventricles, we found that electrical conduction is re-established between existing and regenerated cardiomyocytes between 2 and 4 weeks post-injury. After injury and prolonged fibroblast growth factor receptor inhibition to arrest cardiac regeneration and enable scar formation, experimental release of the signalling block led to gata4 expression and morphological improvement of the injured ventricular wall without loss of scar tissue. Our results indicate that electrically coupled cardiac muscle regenerates after resection injury, primarily through activation and expansion of cardiomyocyte populations. These findings have implications for promoting regeneration of the injured human heart.

Indexed as

AnimalsAnimals, Genetically ModifiedCell ProliferationElectric ConductivityGATA Transcription FactorsGene Expression RegulationHeartMyocytes, CardiacRegenerationZebrafishZebrafish ProteinsGata4 protein, zebrafishGATA Transcription FactorsZebrafish Proteins

Identifiers

PMID20336144
PMCPMC3040215
OpenAlexW2149161770

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.